Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519882(G;T)
Make rs1057519882(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21974678
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs1057519882
dbSNP (classic)rs1057519882
ClinGenrs1057519882
ebirs1057519882
HLIrs1057519882
Exacrs1057519882
Gnomadrs1057519882
Varsomers1057519882
LitVarrs1057519882
Maprs1057519882
PheGenIrs1057519882
Biobankrs1057519882
1000 genomesrs1057519882
hgdprs1057519882
ensemblrs1057519882
geneviewrs1057519882
scholarrs1057519882
googlers1057519882
pharmgkbrs1057519882
gwascentralrs1057519882
openSNPrs1057519882
23andMers1057519882
SNPshotrs1057519882
SNPdbers1057519882
MSV3drs1057519882
GWAS Ctlgrs1057519882
Max Magnitude0
ClinVar
Risk rs1057519882(T;T)
Alt rs1057519882(T;T)
Reference Rs1057519882(G;G)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Malignant melanoma of skin Colorectal Neoplasms Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Pancreatic adenocarcinoma
Variation info
Gene CDKN2A
CLNDBN Adenocarcinoma of stomach Malignant melanoma of skin Colorectal Neoplasms Squamous cell carcinoma of lung Squamous cell carcinoma of the skin Squamous cell carcinoma of the head and neck Pancreatic adenocarcinoma
Reversed 1
HGVS NC_000009.11:g.21974677C>A
CLNSRC
CLNACC RCV000421337.1, RCV000421945.1, RCV000423473.1, RCV000430232.1, RCV000433093.1, RCV000439595.1, RCV000442947.1,